The tandem Crabbé homologation-radical rearrangement of terminal enediynes leads, in a one-pot procedure, to the enantioselective synthesis of six- and seven-membered ring α-aminoesters bearing a quaternary stereocenter based on the phenomenon of memory of chirality.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1039/c2cc17830c | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
One-pot Crabbé homologation-radical cascade cyclisation with memory of chirality.
Chem Commun (Camb)
March 2012
Institut de Chimie Radicalaire (ICR), UMR 7273, Aix-Marseille Université, Faculté de St Jérôme, Avenue Escadrille Normandie-Niemen, 13397 Marseille Cedex 20, France.
The tandem Crabbé homologation-radical rearrangement of terminal enediynes leads, in a one-pot procedure, to the enantioselective synthesis of six- and seven-membered ring α-aminoesters bearing a quaternary stereocenter based on the phenomenon of memory of chirality.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!